EP1222292B1 - Method for regulating transcription of foreign genes in the presence of nitrogen - Google Patents
Method for regulating transcription of foreign genes in the presence of nitrogen Download PDFInfo
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- EP1222292B1 EP1222292B1 EP00965684A EP00965684A EP1222292B1 EP 1222292 B1 EP1222292 B1 EP 1222292B1 EP 00965684 A EP00965684 A EP 00965684A EP 00965684 A EP00965684 A EP 00965684A EP 1222292 B1 EP1222292 B1 EP 1222292B1
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- promoter
- nitrogen
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- expression
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Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
- C12N9/0036—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on NADH or NADPH (1.6)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
- C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
- C12N15/8237—Externally regulated expression systems
- C12N15/8238—Externally regulated expression systems chemically inducible, e.g. tetracycline
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0012—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
- C12N9/0044—Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on other nitrogen compounds as donors (1.7)
Definitions
- the invention relates to a method of regulating the transcription of transgene in genetically-modified organisms. More specifically, the invention relates to the use of expression vectors harboring the coding sequence of a gene of interest under the transcriptional control of promoting sequences for which activity is regulated by the presence of nitrogen.
- these constructs are used in transgenic leguminous plants (for example soybean, alfalfa, clover, birdsfoot trefoil, beans, peas, peanuts) where growth is not impaired by lack of mineral nitrogen, and in which induction of expression could be performed at any given time during development, through the addition of a suitable nitrogen source.
- the invention could be used to induce expression of any given transgene through the addition of any nitrogen source, provided that the organism can be grown adequately in the absence of this nitrogen inducer; as an example within the plant kingdom, duckweed (Lemna minor) can adapt to grow either on nitrate or ammonium as nitrogen source; transgenic duckweed could therefore be grown on nitrate as a sole nitrogen source and expression of the transgene triggered by the addition of ammonium, provided that the cassette contains a promoter from a native gene for which expression is turned on by the addition of ammonium.
- the invention therefore provides a means of regulating the expression of a transgenic trait in any organism through the addition of various nitrogenous inducer.
- Nitrogen is a molecule essential to life. All living organism need nitrogen in order to synthesize amino acids, the building blocks of proteins, and nucleotides, the building blocks of nucleic acids. It is Ammonium nitrate is the preferred form of mineral nitrogen provided to crops in the form of fertilizer. Nitrate-nitrogen is first reduced to nitrite and then to ammonium through the activity of a metabolic pathway common to most herbaceous plants. Depending on the species, part or all of the absorbed nitrate will move to leaf cells through the xylem before it is reduced to ammonium. Ammonium, or other reduced forms of nitrogen are also absorbed (although usually at lower rates) by the root system but their assimilation does not require reduction.
- ammonium or ammonium-containing molecules join the endogenous pools in the cells which is formed by ammonium cycling through amino acids and other nitrogenous molecules.
- Some species do not metabolize nitrate-nitrogen easily and therefore cannot rely on nitrate as sole nitrogen source; many coniferous species fall into this latter category.
- Legumes and other symbiotic plant species form a third large class of nitrogen user within the plant kingdom; they form a metabolic alliance with a microbial organism through which they can fix gaseous nitrogen. This reduced nitrogen is used efficiently by the plant for growth, and therefore, these crops can develop independently of the availability of mineral nitrogen in the soil.
- NaR nitrate reductase
- NiR nitrite reductase
- nitrate is not the only regulatory molecule involved in the control of NaR and NiR expression, its presence is essential to initiate the cascade of transduction that eventually leads to sustained transcription and translation of these genes. It has been shown that expression of NaR and NiR genes is repressed in leguminous plants when they are grown in the absence of mineral nitrogen
- NiR promoters have been characterized in some plant species (Back et al., 1991, Plant Molecular Biology 17 :9-18; Sander et al., 1995, Plant Molecular Biology 27 :165-177). Inducibility of these promoters have also been characterized using marker genes in transgenic plants, where it was shown that availability of nitrate is required for full activation of transcription.
- inducible promoters have been proposed, and in some instances used successfully, to counteract the combined effect of all the above-mentioned factors. Strong inducible promoters may succeed in generating high ephemerous transcription rates which result in high transitory accumulation of foreign mRNA and translational product. As a result, when inducibility of expression is paired with adequate synchronized protein recovery procedures, the yield per unit obtained is higher than with the use of constitutive expression.
- inducible promoters are currently used in plant (wound inducibility) or animal (specificity to cells of the mammary glands, PPL) systems, although none reported are using low-cost and bio-safe chemical inducers such as nitrate salts.
- One aim of the present invention is to provide a method of regulating the transcription of transgene in genetically-modified organisms.
- Another aim of the present invention is to provide the use of expression vectors harboring the coding sequence of a gene of interest under the transcriptional control of promoting sequences for which activity is regulated by the presence of nitrogen.
- the present invention relates to the use of a nitrogen-inducible expression cassettes for the controlled expression of foreign genes in plants. It will be shown from the following description that isolating such a regulatory sequences can be performed so that when cis-acting sequences are appropriately associated to the open reading frame of a gene of interest, its transcription can be controlled by the addition of specific nitrogen sources.
- the targeted system uses leguminous plant species, so that constructs containing a nitrate-inducible promoter will be maintained transcriptionally low throughout the growth period if the transgenic plant is maintained on a nitrate-free medium, thus allowing the development of the plant biomass without interference from the transgenic trait.
- nitrate Upon addition of nitrate to the growth medium, transcription will be induced in a relatively large proportion of the biomass over the following days. Optimization of induction time and protein accumulation will then be performed in order to maximize recovery of the desired recombinant product.
- nitrogen inducibility can also be used to maximize protein production in organisms which do not perform nitrogen fixation through symbiotic association, but that can use variable sources of nitrogen (reduced or oxidized) for growth, and thus possess the ability to develop adequately while one of their nitrogen assimilation pathway is inactive due to lack of one nitrogenous substrate in the growing environment.
- Using an expression cassettes that controls the transcription of any gene in this inactive pathway in order to drive the expression of a gene of interest in such an organism will allow for inducible expression of the transgenic trait upon addition of the previously lacking nitrogenous compound.
- duckweed is a plant species that can grow alternately on nitrate or ammonium; this Invention could be used to develop an expression cassette harboring an ammonium-inducible promoter appropriately linked to a gene of interest so that the induction would be performed on nitrate-grown transgenic duckweed plants.
- the present invention provides an isolated promoter sequence according to claims 1-4 and uses of this promoter sequence according to claims 5-18.
- the cis-acting sequence may be isolated from 5' upstream region of an expressed Nir gene in alfalfa.
- the promoter has the sequence set forth in SEQ ID NO:1 to 13
- the organism is a plant, more preferably a dicotyledonous plant.
- the organism is alfalfa or tobacco.
- the nitrogen inducer is nitrate.
- the organism is a plant, a fungus, a bacteria, a yeast or an animal.
- the cis-acting sequence is isolated from the 5' upstream region of any gene involved in a nitrogen assimilatory pathway.
- the cis-acting sequence is isolated from the 5'upstream region of any gene for which transcription is modulated by availability of a given nitrogen source.
- the cis-acting sequence is any sequence for which transcriptional activity is regulated by addition or removal of any nitrogen source in or from any living organism's environment.
- the organism from which the cis-acting sequence is isolated from is any plant, fungus, yeast, bacteria or animal.
- a promoter for promoting transcription of a foreign gene in transgenic organisms which comprises a nitrogen-inducible promoter with or without cis-acting sequence for expression of said gene and adapted to be modulated for transcriptional expression of said gene by addition or removal of a nitrogen inducer said promoter having the nucleic acid sequence as depicted in SEQ ID No:1 to 13.
- said promoter is used in combination with a terminator which comprises a polyadenylation signal end site for insertion at the 3'end of said gene, wherein said terminator is operationally located with respect to said gene and said promoter and thereby allows expression of said gene.
- the terminator has a sequence selected from the group consisting of SEQ ID NOS: 14 to 16.
- a NiR cDNA strand was first isolated from alfalfa using RT-PCR with primers deduced from a consensus plant NiR sequence. This cDNA stretch was then used either to perform upstream/downstream genome walking. The NiR promoter region and deletions, the 5'UTR and the NiR terminator were then positioned functionnally to control transcription and terminaison of reporter gene GUS. These constructs were inserted into suitable expression vectors for DNA bombardment onto tobacco and alfalfa leaves and for Agrobacterium mediated DNA transfer as described by Desgagair et al. (1995, Plant Cell Tissue Organ Cult. 42 :129-140). These two DNA transfer methods were used to demonstrate that expression of the reporter gene can be modulated by addition or removal of nitrate in the growing medium.
- E. coli strain DH5- ⁇ was used to perform all cloning steps.
- Cold resistant alfalfa genotype 11.9 was used for all experiments including stable transformation using A . tumefaciens infection (Desgagiene et al. (1995, Plant Cell Tissue Organ Cult. 42 :129-140).
- RT-PCR was used to produce a DNA fragment corresponding to one abundant NiR mRNA molecular species from leaf total mRNA.
- a conserved region was first identified from 5 public plant NiR ORFs, namely Genbank sequences #AB006032 (Arabidopsis Nir mRNA), # X66145 (Tobacco partial Nir mRNA), #U10419 (Bean complete Nir cds), #X07568 (Spinach Nir mRNA), and #U90429 (Glycine max Nir complete cds).
- oligonucleotides were deduced from two conserved regions, namely Nir5 - 5' GATATTGATGTTAGACTCAAGTGGC 3' (SEQ ID NO:17), at the 5' end and Nir3 - 5' CACYSATTCCACTTCCTWGGC 3' (SEQ ID NO:18), at the 3' end of the coding strand.
- a reverse transcription reaction was first performed with 200 units of M-MLV reverse transcriptase (RT) for 1 hour at 37°C using 1 ⁇ g of total leaf RNA, 4 mM dNTP (1 mM each), 5 ⁇ M random hexamer primers in a 1X M-MLV-RT buffer (50 mM Tris-HCl pH 8.3, 75 mM KCl, 3mM MgCl 2 ).
- RT M-MLV reverse transcriptase
- the PCR reaction was performed in a Perkin Elmer Cetus GenAmp PCR system 9600 (EG&G, Wellesley, MA), using 2.5 units of Taq DNA polymerase, 2 ⁇ M Nir5 primer, 2 ⁇ M Nir3 primer, 800 ⁇ M dNTPs (200 ⁇ M each) in a 1X PCR buffer (20 mM Tris-HCl pH 8.4, 50 mM KCl, 2 mM MgCl 2 ).
- the cycling program used was: an initial 4 min at 94°C, 30 cycles of 1 min at 94°C, 30 sec at 55°C, and 3 min at 72°C. An extension period of 7 min at 72°C was included in the program.
- DNA sequencing was performed as described by Sanger et al. (1977, P.N.A.S. USA, 74 :5643-5647).
- the amplified 3775 bp fragment was subcloned into pGEM-T Easy vector (Promega, Madison, WI) (Cat #A1360) for further analysis.
- the resulting plasmid was named pGNir4c.
- the downstream walking was performed as the upstream walking using the following NiR specific primers:
- the amplified 3508 bp fragment was subcloned into pGEM-T easy vector (Promega, Madison, WI) (Cat #A1360) for further analysis.
- the resulting plasmid was named pGN3'1.
- the cassettes for expression analysis using the GUS reporter gene were assembled as follows.
- a promoterless GUS cassette was digested from pBI101 with HindIII and EcoRI, and was inserted into the HindIII and EcoRI sites of the pUC19 polycloning site.
- the resulting plasmid was named pBI201 and was used for further constructs.
- the Nir upstream sequences were PCR amplified using the AP2 primer from the Universal Genome Walking Kit as upstream positioned primer, and either one of custom-designed downstream primers ending with a Smal restriction site.
- the 4 primers were positioned either in the 5' UTR region of the gene (Nir-23r-Sma-5'AGAGCCCGGGAGAAGAGAGTGTGTTTG3' (SEQ ID NO:21)), at the end of the transit peptide coding sequence (Nir51r-Sma - 5' TTCTCCCGGGGGACGAGAGATGGATGGT 3' (SEQ ID NO:22)), 50 bp after the transit peptide coding sequence (Nir103r-Sma - 5'TTCTCCCGGGGTTGAA-ACAGGTGCAACTGA 3' (SEQ ID NO:23)), and 100 pb after the transit peptide coding sequence (Nir158r-Sma - 5' TTCTCCCGGGTAACCATCTTTTTCCTCA 3' (SEQ ID NO:24) Amplification was performed under standard conditions with pGNir4c plasmid as template.
- the amplified fragments were digested with specific restriction enzymes in order to produce 5' deletions of the Nir promoter.
- the pNir3k-23 was produced by digesting the fragment previously amplified by AP2 and Nir-23r-Sma primers with Xmal, and inserting the resulting fragment into pBI201 previously digested with Xmal.
- a similar strategy was used to produce the pNir3k51, pNir3k103, and pNir3k158 plasmids except that the downstream primers used were Nir51r-Sma, Nir103r-Sma, and Nir158r-Sma, respectively.
- the pNir2.2k-23 was produced from a SmaI-BgIII digestion of the AP2 - Nir-23-Sma amplified fragment inserted into the pBI201 previously digested with Smal and BamH1.
- the same strategy was used to produce the pNir2.2k51, pNir2.2k103, and pNir2.2k158 plasmids except that the downstream primers used were Nir51r-Sma, Nir103r-Sma, and Nir158r-Sma, respectively. Fidelity and orientation of the insertions were verified by digestion with restriction enzymes.
- deletion fragments were ligated to the 5'terminus of the GUS reporter gene in pBI201, and used for transitory expression studies using DNA bombardment. Upon identification of the adequate deletion fragments, they were sub-cloned into a binary plant expression vector such as pBI101 (Clonetech).
- NiR specific primers were used:
- a 617 bp terminator fragment was PCR amplified using the primers Nir2514c-Sac and Nir3029r-Eco, and a 503 bp terminator fragment was PCR amplified using the primers Nir2728c-Sac and Nir3029r-Eco.
- the fragments obtained were digested with SacI and EcoRI and inserted into the plasmids containing the NiR-GUS constructs after deletion of the NOS terminator between the SacI and EcoRI sites.
- the recombinant plasmids were introduced into Agrobacterium tumefaciens strain LBA4404 by electroporation as described in Khoudi et al (1997, Gene 197 :343-351). Selected Agrobacterium strains were then co-cultivated with leaf disks from genotype C5-1 for 4 days in the absence of selection pressure (kanamycin). Following this incubation period, leaf disks were washed and pampered, and then allowed to form calli onto medium B5H. Calli were then transferred for 21 days on SH medium for embryo induction and for 28 days on BOi2Y for embryo development. Torpedo-shaped embryos were removed from Boi2Y and placed on MS medium for regeneration.
- Kanamycin was present in all cultivation medium except for co-cultivation and regeneration on MS. This method is described in length in Desgagair et al (1995, Plant Cell Tissue Organ Cult . 42 :129-140). Rooted plantlets were grown to maturity in the greenhouse. Integration of the transgene was verified by PCR amplification of a NiR-GUS fragment from genomic DNA. The primers used were:
- the recombinant plasmids were introduced into Agrobacterium tumefaciens strain LBA4404 by electroporation as described in Khoudi et al (1997, Gene 197 :343-351). Selected strains were co-cultivated with leaf disks for 2 days on MS medium without kanamycin. After this period, the explants were transferred to the selection medium (MS with Kanamycin). The explants were kept on this medium for 3 weeks to allow the formation of calli and shoots from the transfected cells. The kanamycin resistant shoots were transferred into the rooting MS medium. Rooted plantlets were grown to maturity in the greenhouse. Integration of the transgene was verified by PCR amplification of a NiR-GUS fragment from genomic DNA. The primer used were:
- Transgenic and non-transgenic tobacco and alfalfa plants were grown in vermiculite medium without nitrate. Mineral balance was kept by repeated additions of nitrate-free Hoagland's solutions (Hoagland and Vamon, 1950, Circular 347 , California Agr. Exp. Stat. Berkeley ) . Nitrate induction was performed by watering the plants with 20-20-20 fertilizer at a concentration of 5gL -1 or as an alternative with Hoagland's solution supplemented with 40 mM nitrate.
- NiR derived promoters were placed upstream of the GUS reporter gene in transcriptional and translational fusions.
- the 5' deletions of the NiR promoter analyzed here consisted in (1) a putative full length promoter comprising 2813 bp upstream of the initial ATG of the coding region, (2) a 1905 bp version of the promoter, and (3) a shorter 1111 bp version of the promoter.
- the 3' end of the promoter was fused to the 5' end of the GUS coding region to form transcriptional and translational fusions.
- Fig. 1 presents the median level of ⁇ -glucuronidase activity measured in the 1 st expanded leaf of plantlets.
- NiR derived promoters showed reactivity to nitrate induction. Between 5 and 10 fold increase of ⁇ -glucuronidase expression was generally observed, irrespectively of the promoter truncation, indicating that important nitrate responsive elements are contained within the first 1.1 kb upstream of the initial ATG. Both 5' and 3' deletions of the NiR promoter led to important modifications of ⁇ -glucuronidase activity. The highest level of GUS expression was obtained with the 2.8 kb promoter, indicating that the far upstream regions have a regulatory role for the level of NiR expression in the leaves.
- the translational fusions of the promoter to the GUS coding region resulted in variable expression level depending on the extension of the 5' end of the promoter.
- the shortest fusion (containing the 17 a.a. NiR transit peptide fused to the amino-terminal end of the ⁇ -glucuronidase) constantly resulted in the highest level of activity for all three 5' end truncations.
- This short translational fusion combined with the longest extension of upstream promoter regions gave rise to the strongest promoter (3kb+50).
- this specific construct resulted in more than 13-fold the level of GUS expression obtained with the 35S-GUS-NOS construct.
- the transcriptional fusion to the GUS gene (3kb-5) was ⁇ 7 times less effective than the short translational fusion (3kb+50).
- the level of GUS expression in the plants harboring the 3kb-5 promoter deletion was more than 1,8-fold that observed in the 35S-GUS-NOS plants.
- Tobacco plants were transformed with constructs consisting of promoter NiR and deletions (SEQ ID NOS: 2, 3, 5 and 6), and 35S, together with 3'UTR sequences and terminator (SEQ ID NOS: 15 and 16), functionally positioned to drive transcription and termination of reporter gene GUS.
- Growth, nitrate induction and GUS activity measurements were performed as per experiment illustrated in Fig 1.
- Results shown in Fig 2 demonstrate that the terminator sequence of Nir allows termination of transcription into a translatable messenger RNA.
- Transgenic alfalfa plant containing the gene constructs presented in Fig. 3 were obtained using the Agrobacterium -mediated transfection method of Desgagair et al. (1995, Plant Cell Tissue Organ Cult. 42 :129-140). The in vitro plants were transferred into growth chamber to allow a normal vegetative growth. Cuttings from each transgenic line were grown in vermiculite and fertilized with nitrate-free Hoagland medium. After two weeks, the roots were inoculated with Nitragin (LiphaTech inc., Milwaukee, WI). Two weeks after inoculation, nodules had developed on the roots.
- Nitragin Nitragin
- Nodulated plants were allowed to continue their vegetative growth for at least another week before the fluorometric measurement of ⁇ -glucuronidase activity (before induction) was performed. After the measurement, the plants were watered with Hoagland medium containing 40 mmol KNO 3 . Two days after induction, leaf ⁇ -glucuronidase activity was measured to evaluate the nitrate inducibitity of the NiR promoter in alfalfa leaves. Results are presented in Fig. 3. Results show that promoter NiR induces expression of GUS reporter gene upon addition of nitrate in nodulated alfalfa plants. Taken together, this last series of result demonstrate that NiR promoter inducibility can be used to positively regulate expression of a foreign gene in alfalfa plants when fixation of atmospheric nitrogen is replaced by nitrate assimilation.
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US4997930A (en) * | 1989-03-16 | 1991-03-05 | Ciba-Geigy Corporation | Cloning of complementary DNA encoding maize nitrite reductase |
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CN1377419A (zh) | 2002-10-30 |
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WO2001025454A3 (en) | 2001-11-08 |
JP2003512821A (ja) | 2003-04-08 |
PT1222292E (pt) | 2005-11-30 |
CA2385347A1 (en) | 2001-04-12 |
US6420548B1 (en) | 2002-07-16 |
BR0014480A (pt) | 2002-06-11 |
WO2001025454A2 (en) | 2001-04-12 |
CA2385347C (en) | 2009-12-15 |
CN100427603C (zh) | 2008-10-22 |
ES2248127T3 (es) | 2006-03-16 |
KR100797667B1 (ko) | 2008-01-23 |
NZ517906A (en) | 2003-01-31 |
DE60022369D1 (de) | 2005-10-06 |
EP1222292A2 (en) | 2002-07-17 |
AU7635800A (en) | 2001-05-10 |
AU782626B2 (en) | 2005-08-18 |
KR20020057967A (ko) | 2002-07-12 |
ATE303445T1 (de) | 2005-09-15 |
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